排序方式: 共有16条查询结果,搜索用时 203 毫秒
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Maxim N. Sokolov Natalia E. Fedorova Eugenia V. Peresypkina Richard Pätow Dieter Fenske 《Inorganica chimica acta》2005,358(13):3914-3918
Two new Re(III) and Re(IV) complexes with 2(2′-pyridyl)benzimidazole (pbimz) were prepared and their crystal and molecular structures established by single-crystal X-ray diffraction. Reaction of [ReOCl2(OEt)(PPh3)2] with the ligand gave red cis(Cl),trans(P)-[ReCl2(PPh3)2(pbimz)]Cl (1), while red [ReCl4(pbimz)] · OPPh3 (2) was obtained from [ReCl3(PhC(O)C(O)Ph)(PPh3)] and pbimz in the presence of perchlorate. The compounds were characterized by elemental analysis, FAB-MS, UV-Vis, IR, NMR spectroscopy and magnetic susceptibility measurements. 相似文献
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Mark B. Bushuev Eugenia V. Peresypkina Alexander V. Virovets Oleg P. Shkurko 《Inorganica chimica acta》2011,365(1):384-390
A series of copper(II) complexes, i.e. Cu2LCl4, CuLCl2·H2O and [Cu2L2Cl4]·2MeCN (8), based on a new potentially polytopic ligand, 3,5-bis(4,6-dimethylpyrimidin-2-yl)-4H-1,2,4-triazol-4-amine (3b, L), have been synthesized. The crystal structures of L and [Cu2L2Cl4]·2MeCN were studied by X-ray single crystal analysis. The dinuclear compound [Cu2L2Cl4]·2MeCN represents the first example of structurally characterized metal complexes with 3,5-di(pyrimidin-2-yl)-4H-1,2,4-triazol-4-amines. Both copper atoms have distorted tetragonal-pyramidal 3N + 2Cl environment. Surprisingly, in contrast to the complexes based on 3,5-di(pyridin-2-yl)-4H-1,2,4-triazol-4-amine (pyridinyl analog of L), the compound [Cu2L2Cl4]·2MeCN adopts a dinuclear trans-(N′,N1,N2)2 double bridging binding mode which is due to tridentate coordination of two L molecules linking two copper atoms through N1,N2-triazole and N′-pyrimidine atoms. It seems to be reasonable that it is methyl groups in pyrimidinyl moiety that obstruct the expected dinuclear (N′,N1,N2,N″)2 double bridging coordination being one of the most common for 4-substituted 3,5-di(pyridin-2-yl)-4H-1,2,4-triazoles and 3,5-di(pyridin-2-yl)-1,2,4-triazolates. Due to π-π stacking interactions, molecules of Cu2L2Cl4 in the structure of [Cu2L2Cl4]·2MeCN form 1D chains. 相似文献
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DAVID G. GARBUZ OLGA G. ZATSEPINA ANDREY A. PRZHIBORO IRINA YUSHENOVA IRINA V. GUZHOVA MICHAEL B. EVGEN’EV 《Molecular ecology》2008,17(21):4763-4777
A population of Stratiomys japonica, a species belonging to the family Stratiomyidae (Diptera), common name ‘soldier flies’, occurs in a hot volcanic spring, which is apparently among the most inhospitable environments for animals because of chemical and thermal conditions. Larvae of this species, which naturally often experience temperatures more than 40 °C, have constitutively high concentrations of the normally inducible heat-shock protein Hsp70, but very low level of corresponding mRNA. Larvae of three other species of the same family, Stratiomys singularior, Nemotelus bipunctatus and Oxycera pardalina, are confined to different type semi-aquatic habitats with contrasting thermal regime. However, all of them shared the same pattern of Hsp70 expression. Interestingly, heat-shock treatment of S. japonica larvae activates heat-shock factor and significantly induces Hsp70 synthesis, whereas larvae of O. pardalina, a species from constant cold environment, produce significantly less Hsp70 in response to heat shock. Adults of the four species also exhibit lower, but detectable levels of Hsp70 without heat shock. Larvae of all species studied have very high tolerance to temperature stress in comparison with other Diptera species investigated, probably representing an inherent adaptive feature of all Stratiomyidae enabling successful colonization of highly variable and extreme habitats. 相似文献
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The phylogeny of selected genera from four subfamilies of fungus gnats (Diptera: Mycetophilidae) – Manotinae, Leiinae, Sciophilinae and Gnoristinae (including Metanepsiini) – is reconstructed based on the combined analysis of five mitochondrial (12S, 16S, COI, COII, cytB) and two nuclear (28S, ITS2) gene markers. Results of the different analyses all support Manotinae as a monophyletic group, with Leiinae as the sister group. Allactoneura DeMeijere is nested in the monophyletic and strongly supported clade of Leiinae. The tribe Metanepsiini is revealed as paraphyletic and the genera Metanepsia Edwards and Chalastonepsia Søli do not appear to be closely related. The genera Docosia Winnertz, Ectrepesthoneura Enderlein, Novakia Strobl and Syntemna Winnertz were placed with a group of genera included traditionally in the Gnoristinae. The monophyly of Dziedzickia Johannsen and Phthinia Winnertz is not supported. The genera of Sciophilinae (excluding Paratinia Mik but including Eudicrana Loew) form a monophyletic group in the Bayesian model. 相似文献
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JEAN‐CLAUDE WALSER MICHAEL B. EVGENEV MARTIN E. FEDER 《Molecular ecology resources》2006,6(2):563-567
We adapted a recently developed nonrestrictional, nonligational genome walking method, Universal Fast Walking (UFW), for detection of length polymorphism in the proximal promoter region of genes. We demonstrate its efficacy at discovering naturally occurring transposition into heat‐shock genes of wild Drosophila and show that it surmounts limitations of simple polymerase chain reaction (PCR) approaches. We further present modifications to the standard UFW protocol and provide some guidelines to improve specificity. Although the resultant banding pattern of a standard UFW can be regarded as a DNA fingerprint, many amplicons result from false priming and not real polymorphisms. We describe ways to distinguish between UFW amplicons and false priming products in a high‐throughput assay. 相似文献
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P.A. Abramov M.N. Sokolov E.V. Peresypkina N.K. Moroz R. Hernandez-Molina M.C. Arévalo 《Inorganica chimica acta》2011,375(1):314-319
New cluster complex [Mo3SeO3(acac)3(py)3]+ was obtained by ligand substitution in the aqua complex [Mo3SeO3(H2O)9]4+. Crystal structure was determined for [Mo3SeO3(acac)3(py)3]PF6·C6H5CH3. The complex was characterized by 77Se NMR, electrospray mass-spectrometry, and cyclic voltammetry. DFT calculations were used to confirm the assignment of chemical shift and to study Mo-Mo bonding in the cluster core. 相似文献